POLG Pathogenicity Prediction Server

1 patient data entry in database for mutations P587L and R853Q.

Entry
#

Mutations
allele 1	allele 2

Clinical representation

Symptoms

Age group

Age of onset

Age of patient

Age of death

Reference

R853Q1

T251I
P587L2

Developmental delay, dementia, lactic acidosis, microcephaly, FTT, hearing loss, abnormal MRI.

-	lactic acidosis

-	failure to thrive

-	developmental delay

dementia

-	microcephaly

-	hearing loss

infantile

n/a

0.2

n/a

Wong et al, 2008;

[view data]

^1-5 pathogenic cluster assignment of mutations. Mutations displayed without a superscript number are outside of the assigned pathogenic clusters. See cluster definitions for details.

Search criteria for patient entries:

Mutations Entry IDs Clusters Reference Residue range

Reference:

References in full format are accessible through the references page.

Mutations:

Allele 1:	Allele 2:

Separate multiple mutations with commas. Use "PNF" for non-missense mutations.

Match: Inclusive Exact

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